Canonical Allele Identifier: CA118945733
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs981364876
gnomAD v3: 5-55233621-T-C
gnomAD v4: 5-55233621-T-C
MyVariant Identifiers: chr5:g.54529449T>C (hg19) chr5:g.55233621T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233621T>C , CM000667.2:g.55233621T>C GRCh38
NC_000005.9:g.54529449T>C , CM000667.1:g.54529449T>C GRCh37
NC_000005.8:g.54565206T>C NCBI36
NG_034201.1:g.5097A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-98A>G ENSP00000282572.4:n.-98A>G
NM_021147.4:c.-98A>G NP_066970.3:n.-98A>G
NR_125346.1:n.97A>G
NR_125347.1:n.97A>G
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